As a Formulation and Process Development Scientist, you will be responsible for the formulation and process development of Solid Orals, Liquid Orals, and Semi Solids dosage forms. Your main tasks will include designing protocols and development plans for new products, conducting formulation trials, and evaluating stability data to finalize formulation compositions. You will also be involved in tentative costing Bill of Materials (BOM) and trial BOM preparation for trial execution. Additionally, you will prepare supporting documents for stability studies, resolve product stability issues, and develop manufacturing processes for R&D formulations to ensure successful technical transfer for large-scale batches. Your role will also involve writing master formulas, manufacturing procedures, stability protocols, and validation reports, as well as supporting technology transfer for manufacturing processes from laboratory scale to production scale. Furthermore, you will be responsible for developing FSSAI / AYUSH, EU, and US FDA compliant Supplement Facts and Nutrition Facts labels from product formulas. You will also create and review production Master Formula records and Manufacturing batch Records. The ideal candidate for this position should have 5-6 years of relevant experience in formulation and process development. If you are a detail-oriented professional with a strong background in pharmaceutical development and regulatory compliance, we encourage you to apply for this exciting opportunity.,
As a Regulatory Executive at ATS Consultancy in Noida, your role will involve overseeing and ensuring compliance with regulatory requirements. This includes conducting audits, preparing and submitting regulatory documents, and effectively communicating with regulatory agencies. Key Responsibilities: - Overseeing and ensuring compliance with regulatory requirements - Conducting audits to assess regulatory compliance - Preparing and submitting regulatory documents to relevant authorities - Communicating effectively with regulatory agencies Qualifications: - Knowledge of regulatory requirements and standards - Experience in conducting audits and preparing regulatory documents - Strong attention to detail and organizational skills - Excellent written and verbal communication skills - Ability to work collaboratively in a team environment - Experience in the pharmaceutical or healthcare industry is a plus - Bachelor's degree in a relevant field such as Regulatory Affairs, Life Sciences, or Pharmacy,